Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
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DOID:9870 | galactosemia | MGI:95638 | Mus musculus (house mouse) | 14430 | Galt |
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DOID:0080467 | developmental and epileptic encephalopathy 2 | MGI:1278336 | Mus musculus (house mouse) | 382253 | Cdkl5 |
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DOID:9352 | type 2 diabetes mellitus | MGI:1921765 | Mus musculus (house mouse) | 68916 | Cdkal1 |
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DOID:0080720 | autosomal dominant congenital deafness with onychodystrophy | MGI:109618 | Mus musculus (house mouse) | 11966 | Atp6v1b2 |
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DOID:0110320 | hypertrophic cardiomyopathy 14 | MGI:97255 | Mus musculus (house mouse) | 17888 | Myh6 |
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DOID:0110552 | autosomal dominant nonsyndromic deafness 22 | MGI:104785 | Mus musculus (house mouse) | 17920 | Myo6 |
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DOID:2841 | asthma | MGI:105367 | Mus musculus (house mouse) | 16190 | Il4ra |
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DOID:0060316 | orofaciodigital syndrome I | MGI:1350328 | Mus musculus (house mouse) | 237222 | Ofd1 |
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DOID:14693 | Clouston syndrome | MGI:107588 | Mus musculus (house mouse) | 14623 | Gjb6 |
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DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | MGI:1346525 | Mus musculus (house mouse) | 24052 | Sgcd |
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DOID:0060697 | hyperekplexia 2 | MGI:95751 | Mus musculus (house mouse) | 14658 | Glrb |
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DOID:0111671 | primary hyperoxaluria type 2 | MGI:1923488 | Mus musculus (house mouse) | 76238 | Grhpr |
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DOID:0060439 | lysinuric protein intolerance | MGI:1337120 | Mus musculus (house mouse) | 20540 | Slc7a7 |
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DOID:0110142 | Bartter disease type 1 | MGI:103150 | Mus musculus (house mouse) | 20495 | Slc12a1 |
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DOID:0110377 | retinitis pigmentosa 49 | MGI:88436 | Mus musculus (house mouse) | 12788 | Cnga1 |
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DOID:0050790 | fibular hypoplasia and complex brachydactyly | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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DOID:0060462 | Desbuquois dysplasia | MGI:1923275 | Mus musculus (house mouse) | 76025 | Cant1 |
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DOID:9119 | acute myeloid leukemia | MGI:96680 | Mus musculus (house mouse) | 16653 | Kras |
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DOID:0110033 | autosomal recessive Alport syndrome | MGI:104688 | Mus musculus (house mouse) | 12828 | Col4a3 |
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DOID:0080312 | neurodevelopmental disorder with midbrain and hindbrain malformations | MGI:103264 | Mus musculus (house mouse) | 16800 | Arhgef2 |
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DOID:0060041 | autism spectrum disorder | MGI:1930016 | Mus musculus (house mouse) | 58234 | Shank3 |
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DOID:0050545 | visceral heterotaxy | MGI:2664387 | Mus musculus (house mouse) | 214766 | Mmp21 |
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DOID:0110858 | polycystic kidney disease 1 | MGI:97603 | Mus musculus (house mouse) | 18763 | Pkd1 |
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DOID:12930 | dilated cardiomyopathy | MGI:97255 | Mus musculus (house mouse) | 17888 | Myh6 |
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DOID:0110218 | Brugada syndrome 1 | MGI:98251 | Mus musculus (house mouse) | 20271 | Scn5a |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024